Canonical Allele Identifier: CA402046467

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478780T>G (hg19) ; chr18:g.23898816T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898816T>G , CM000680.2:g.23898816T>G	GRCh38
NC_000018.9:g.21478780T>G , CM000680.1:g.21478780T>G	GRCh37
NC_000018.8:g.19732778T>G	NCBI36
NG_007853.2:g.214219T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.865T>G MANE Plus Clinical	ENSP00000269217.5:p.Leu289Val
ENST00000313654.14:c.5692T>G MANE Select	ENSP00000324532.8:p.Leu1898Val
ENST00000649721.1:c.2584T>G	ENSP00000497885.1:p.Leu862Val
ENST00000269217.10:c.865T>G	ENSP00000269217.5:p.Leu289Val
ENST00000313654.13:c.5692T>G	ENSP00000324532.8:p.Leu1898Val
ENST00000399516.7:c.5692T>G	ENSP00000382432.2:p.Leu1898Val
ENST00000586709.1:n.80T>G
ENST00000586751.5:c.470T>G
ENST00000587184.5:c.865T>G	ENSP00000466557.1:p.Leu289Val
ENST00000588770.5:n.270T>G
NM_000227.4:c.865T>G	NP_000218.3:p.Leu289Val
NM_001127717.2:c.5692T>G	NP_001121189.2:p.Leu1898Val
NM_001127718.2:c.865T>G	NP_001121190.2:p.Leu289Val
NM_198129.2:c.5692T>G	NP_937762.2:p.Leu1898Val
XM_011525978.1:c.5719T>G	XP_011524280.1:p.Leu1907Val
XM_011525979.1:c.5710T>G	XP_011524281.1:p.Leu1904Val
XM_011525980.1:c.5701T>G	XP_011524282.1:p.Leu1901Val
XM_011525981.1:c.5587T>G	XP_011524283.1:p.Leu1863Val
XM_011525982.1:c.5719T>G	XP_011524284.1:p.Leu1907Val
XM_011525978.2:c.5719T>G	XP_011524280.1:p.Leu1907Val
XM_011525979.2:c.5710T>G	XP_011524281.1:p.Leu1904Val
XM_011525980.2:c.5701T>G	XP_011524282.1:p.Leu1901Val
XM_011525981.2:c.5587T>G	XP_011524283.1:p.Leu1863Val
XM_011525982.2:c.5719T>G	XP_011524284.1:p.Leu1907Val
XM_017025743.1:c.3571T>G	XP_016881232.1:p.Leu1191Val
XM_017025744.1:c.1261T>G	XP_016881233.1:p.Leu421Val
XR_001753199.1:n.5960T>G
NM_000227.5:c.865T>G	NP_000218.3:p.Leu289Val
NM_001127717.3:c.5692T>G	NP_001121189.2:p.Leu1898Val
NM_001127718.3:c.865T>G	NP_001121190.2:p.Leu289Val
NM_198129.3:c.5692T>G	NP_937762.2:p.Leu1898Val
NM_000227.6:c.865T>G MANE Plus Clinical	NP_000218.3:p.Leu289Val
NM_001127717.4:c.5692T>G	NP_001121189.2:p.Leu1898Val
NM_001127718.4:c.865T>G	NP_001121190.2:p.Leu289Val
NM_198129.4:c.5692T>G MANE Select	NP_937762.2:p.Leu1898Val